- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06031571
Effect of Dynamic Cupping Versus Myofascial Release Therapy in Patients With Mechanical Neck Pain
Effect of Dry Cupping Massage Versus Myofascial Release Therapy in Patients With Mechanical Non-specific Neck Pain: a Quasi-experimental Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
PURPOSE: To investigate the effect of dry cupping massage versus myofascial release on pain level, range of motion, and functional level in mechanical neck pain…
BACKGROUND: Neck pain is a multivariate disease and is a leading issue in a modernized society. The economic burden of neck pain is remarkable and includes treatment costs, reduced productivity, and job-related problems (Cohen, 2015).
There is no one definitive treatment for neck pain. However, different pharmacological and non-pharmacological treatments have been recommended, including laser therapy, massage, acupuncture, yoga, and aquatic therapy (Corvillo et al., 2020). However, no studies are focusing on comparing the effect of dynamic cupping and myofascial release in mechanical neck pain.
HYPOTHESES: There will be a non-significant difference between dry cupping massage and myofascial release on pain level, range of motion, and functional level in patients with mechanical neck pain…
RESEARCH QUESTION: Will there be a difference between dry cupping massage versus myofascial release on pain level, range of motion, and functional level in patients with mechanical neck pain?
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Cairo, Egypt, 82798
- Recruiting
- Faculty of Physical Therapy
-
Contact:
- Mohamed G Shehata
- Phone Number: 01014397608
- Email: dr_m.gamal1987@svu.edu.eg
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-
Qena
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Qinā, Qena, Egypt, 83523
- Recruiting
- Faculty of physical therapy, South Valley University
-
Contact:
- Mohamed GA Ali, Lecturer
- Phone Number: +201001441982 +201014397608
- Email: dr_m.gamal1987@svu.edu.eg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 18- 40 years.
- Participants have experienced mechanical neck pain for at least the previous 3 months.
Exclusion Criteria:
- Participants aged below 18 years-old and those above 40 years old
- Mechanical neck pain due to trauma, disc protrusion, congenital deformity of the spine, spinal stenosis, and rheumatoid disease.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: group A
group A (will receive cupping massage technique in addition to traditional exercises)
|
Dry cupping is a form of massage therapy that involves using Hijamat cups without skin injury while applying suction and then performing circular and transverse movements
Other Names:
|
|
Experimental: Group B
group B (will receive myofascial release technique in addition to traditional exercises)
|
Myofascial release is a form of manual therapy using hands-on techniques to regain tissue extensibility and elasticity
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical range of motion
Time Frame: Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
|
Cervical flexion and extension ranges of motion are measured by goniometer in numerical degrees
|
Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neck Disability index
Time Frame: Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
|
The neck disability index is a questionnaire has been designed to inform how neck pain has affected different aspects in everyday life.
|
Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
|
|
Visual analog scale
Time Frame: Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
|
The visual analog scale is a scale for pain severity assessment with range from 0 (o pain) to 10 (intolerable pain)
|
Assessment will be done pre and post treatment sessions (3 sessions/week, total of 12 sessions in 4 weeks)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- cupping vs release
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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